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The Effect of New Zealand Blackcurrant (NZBC) Supplementation on Recovery Following Strenuous Exercise

The Effect of New Zealand Blackcurrant (NZBC) Supplementation on Indices of Muscle Damage Following Strenuous Exercise

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05010057
Acronym
CurraNZ_MD
Enrollment
27
Registered
2021-08-18
Start date
2016-06-10
Completion date
2018-09-01
Last updated
2021-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Damage

Keywords

Exercise-induced muscle damage, Recovery, Supplementation, Oxidative stress, Anthocyanin, New Zealand blackcurrant

Brief summary

The study aims to examine the effect of a New Zealand blackcurrant (NZBC) supplement on markers of muscle damage and recovery following strenuous resistance exercise. The investigation will compare responses between an experimental (NZBC capsule, 300 mg/day) and placebo (PLA capsule, 300 mg sugar) group. Participants will attend a screening session where they will consent to the study, complete a pre-activity medical questionnaire and have their height, weight and resting blood pressure measured. If the participants meet the inclusion criteria they will perform a familarisation session on the muscle strength assessment. Participants will be randomized to NZBC or placebo groups, and consume one capsule in the morning (between 6-10 am) for 12 days. This is a double-blinded study, which means that the participant and the study team will not know which group the participants are assigned to until the study is over. On day 8 participants will perform a strenuous bout of upper body resistance exercise on the isokinetic dynamometer (exercise device). Muscle strength and soreness, arm circumference, and elbow range of motion will be measured, and a fasted blood sample will be collected, before and 24, 48, 72 & 96 hours after the muscle fatigue protocol (on days 9, 10, 11 & 12). A marker of muscle damage (creatine kinase \[CK\] concentration) will be measured in the blood samples. Participants will also be asked to complete a 6-day dietary record, beginning on day 7 and ending on the final day of testing (day 12).

Interventions

DIETARY_SUPPLEMENTNew Zealand blackcurrants (NZBC)

NZBC capsules containing anthocyanin-rich blackcurrant extract

DIETARY_SUPPLEMENTPlacebo (PLA)

Placebo capsules containing microcrystalline cellulose

Sponsors

University of Surrey
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Masking description

Coded, capsules

Intervention model description

Randomised, parallel design.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Males and Females * 18 - 45 years old * BMI: 19 - 29.9 kg/m2 * Healthy: no active disease process that could interfere with endpoints measured as determined by medical history

Exclusion criteria

* Smoking and tobacco use * Takes medication \[excluding contraception\] * BMI ≥ 30 kg/m2 * Hypertensive (diastolic \> 90 and/or systolic blood pressure \> 140 mmHg) * History of musculoskeletal upper limb injuries * Performs regular resistance exercise (\> 2 sessions per week) * Uses dietary supplements that could influence muscle recovery or function (e.g. protein supplements, antioxidants etc)

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in creatine kinase (CK) concentration at 72 hours post-exerciseAt baseline (pre-exercise) and 72 hours post-exercise.Serum biomarker for muscle damage
Change from baseline in creatine kinase (CK) concentration at 96 hours post-exerciseAt baseline (pre-exercise) and 96 hours post-exercise..Serum biomarker for muscle damage

Secondary

MeasureTime frameDescription
Change in maximum voluntary contraction (MVC) from baseline to 96 hours post-exerciseAt baseline (pre-exercise) and post-exercise time points (at 0, 24, 48, 72 and 96 hours respectively).Muscle function measure; maximal voluntary isometric contraction (torque, Nm) performed on isokinetic dynamometer
Change in rating of Delayed Onset of Muscle Soreness (DOMS) from baseline to 96 hours post-exerciseAt baseline (pre-exercise) and post-exercise time points (at 24, 48, 72 and 96 hours respectively).Self-reported perception of muscle soreness using a visual analogue scale (VAS), from 'no soreness' \[0 mm\] on the left anchor point to 'extremely sore' \[100 mm\] on the right
Change in joint range of motion (ROM) from baseline to 96 hours post-exerciseAt baseline (pre-exercise) and post-exercise time points (at 24, 48, 72 and 96 hours respectively).Elbow ROM measured using a goniometer
Change in mid arm circumference (MAC) from baseline to 96 hours post-exerciseAt baseline (pre-exercise) and post-exercise time points (at 24, 48, 72 and 96 hours respectively).Mid-upper arm circumference measured at the midpoint of the distance from the acromion process (acromiale) to the olecranon process (radiale).

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026